Exosome component 3

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Exosome component 3

Exosome component 3, also known as EXOSC3, is a human gene, which is part of the exosome complex.[5]

Quick Facts EXOSC3, Available structures ...
EXOSC3
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesEXOSC3, PCH1B, RRP40, Rrp40p, bA3J10.7, hRrp-40, p10, CGI-102, Exosome component 3
External IDsOMIM: 606489; MGI: 1913612; HomoloGene: 6867; GeneCards: EXOSC3; OMA:EXOSC3 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_016042
NM_001002269

NM_025513
NM_001362788

RefSeq (protein)

NP_001002269
NP_057126

NP_079789
NP_001349717

Location (UCSC)Chr 9: 37.76 – 37.83 MbChr 4: 45.32 – 45.34 Mb
PubMed search[3][4]
Wikidata
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Clinical significance

Mutations in EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degeneration.[6]

References

Further reading

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